Product image of Liferol (Formoterol Fumarate Dihydrate) supplied by GNH India

Liferol

Active Ingredient:
Formoterol Fumarate Dihydrate
Origin:
EU

Liferol (Formoterol Fumarate Dihydrate)

Formoterol Fumarate Dihydrate, the active ingredient in Liferol, is a long‑acting β2‑adrenergic agonist (LABA) presented as an inhalation product for inhalation use. It provides sustained bronchodilation to help manage asthma and chronic obstructive pulmonary disease (COPD) in adult patients, improving airflow and reducing symptom frequency.

GNH India supplies Liferol as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company follows European Union manufacturing standards, provides full regulatory documentation, and offers reliable global logistics for bulk and parcel orders.

Manufacturer / TM Owner

Master Pharma S.R.L.

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Indications & Clinical Uses

Formoterol is a long‑acting β2‑adrenergic agonist used in maintenance therapy for obstructive airway diseases.

  • Asthma (maintenance therapy): improves airway patency, reduces frequency of symptoms and exacerbations.
  • Chronic obstructive pulmonary disease (COPD): enhances lung function, decreases rescue medication use and lowers risk of exacerbations.
  • Exercise‑induced bronchoconstriction (prevention): provides sustained bronchodilation to help prevent airway narrowing during physical activity.

How It Works

  • Formoterol binds selectively to β2‑adrenergic receptors on airway smooth‑muscle cells, activating adenylate cyclase and increasing intracellular cyclic AMP. The rise in cAMP leads to protein kinase A activation, which phosphorylates target proteins causing relaxation of smooth‑muscle fibers and inhibition of mediator release, resulting in prolonged bronchodilation lasting up to 12 hours. The drug’s high intrinsic efficacy and lipophilicity allow it to remain bound to the receptor, providing sustained action with minimal tachyphylaxis.

Side Effects

Formoterol may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Tremor: mild muscle shaking, often transient.
  • Headache: dull or throbbing head pain.
  • Throat irritation: discomfort or soreness in the throat.
  • Cough: transient cough after inhalation.

Serious or Rare Side Effects

  • Paradoxical bronchospasm: sudden worsening of breathing requiring immediate medical attention.
  • Cardiac arrhythmias: irregular heartbeats, palpitations, or tachycardia.
  • Hypersensitivity reactions: rash, angioedema, or anaphylaxis.
  • Low potassium (hypokalemia): may occur especially with concomitant diuretics.

Precautions & Warnings

When prescribing or dispensing Formoterol, several safety considerations should be observed.

  • Dose titration: follow the prescriber’s instructions and adjust based on clinical response.
  • Monitor lung function: assess spirometry or peak flow regularly to ensure efficacy.
  • Avoid monotherapy for acute relief: do not use Formoterol alone as a rescue inhaler.
  • Cardiovascular caution: use carefully in patients with arrhythmias, hypertension, or coronary disease.
  • Pregnancy and lactation: risk category unknown; discuss potential benefits and risks with a healthcare professional.
  • Store at room temperature: keep in the original container, protect from moisture and direct heat.

Avoid Interactions

Formoterol can interact with other medicines, influencing its bronchodilator effect or increasing adverse event risk.

Major Interactions (Avoid)

  • Beta‑blockers: may antagonize bronchodilation and precipitate bronchospasm.
  • MAO inhibitors: can enhance cardiovascular stimulation, raising the risk of tachycardia.

Moderate Interactions (Monitor Closely)

  • Diuretics: may increase the likelihood of hypokalemia when combined with Formoterol.
  • Theophylline: concurrent use can raise the chance of tremor and tachycardia.
  • Other LABAs or long‑acting bronchodilators: additive effects may increase risk of cardiovascular side effects.

Frequently Asked Questions

Liferol contains formoterol fumarate, a long‑acting β2‑adrenergic agonist that is prescribed for maintenance treatment of asthma and chronic obstructive pulmonary disease (COPD). It helps keep the airways open by providing sustained bronchodilation, reducing symptoms such as wheezing, shortness of breath, and the need for rescue medication.

Formoterol selectively stimulates β2‑adrenergic receptors on airway smooth‑muscle cells, activating adenylate cyclase and raising cyclic AMP levels. The increased cAMP activates protein kinase A, which relaxes smooth‑muscle fibers and inhibits release of bronchoconstrictive mediators, resulting in prolonged widening of the airways.

The specific dose and inhalation schedule for Liferol are determined by the prescribing clinician based on the patient’s condition, severity, and response to therapy. Dosage instructions are individualized and should be followed exactly as written on the prescription label.

Formoterol’s pregnancy category is not definitively established. It should only be used during pregnancy or while breastfeeding if the potential benefit justifies any potential risk to the fetus or infant. Healthcare providers should evaluate each case and discuss possible alternatives.

To request Liferol, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and the necessary import documentation.

Liferol (formoterol) is a long‑acting β2‑agonist that offers a rapid onset of action and up to 12‑hour bronchodilation, distinguishing it from some other LABAs that may have slower onset. Compared with short‑acting agents, it is not intended for immediate symptom relief but provides sustained control when used regularly.

Store Liferol at room temperature, typically below 25 °C. Keep the inhaler in its original packaging, protect it from moisture, direct sunlight, and excessive heat. Do not expose the product to freezing temperatures, as this could affect the integrity of the formulation.

Liferol is administered by inhalation using a metered‑dose inhaler or a compatible dry‑powder device, as directed by the prescriber. The patient should inhale the dose fully, hold their breath for a few seconds, and then exhale slowly. Proper technique should be reviewed with a healthcare professional.

Serious risks include paradoxical bronchospasm, which can worsen breathing, and cardiovascular effects such as tachycardia, arrhythmias, or hypertension. Rarely, hypersensitivity reactions like rash, angioedema, or anaphylaxis may occur. Patients should seek immediate medical attention if they experience severe breathing difficulty or chest pain.

Liferol should be avoided in patients with known hypersensitivity to formoterol or any component of the inhaler. It is also contraindicated for individuals who require a rapid‑acting bronchodilator for acute symptom relief only, as it is not intended for rescue therapy. Clinicians should assess cardiovascular status before initiating treatment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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